ALBERT

Beschreibung: PM10 and size-resolved particles (9-stage) were simultaneously collected at Mt. Hua and Mt. Tai in central and east China during the spring of 2009 including a massive dust storm occurring on 24 April (named as DS II), and determined for organic compounds to investigate the impact of dust storm on organic aerosols. High molecular weight (HMW) n-alkanes, fatty acids, and fatty alcohols and trehalose sharply increased and almost entirely stayed in coarse particles when dust storm was present, suggesting that high level of organic aerosols in the mountain atmospheres during the event largely originated from Gobi desert plants. However, most anthropogenic aerosols (e.g. PAHs, and aromatic and dicarboxylic acids) during the event significantly decreased due to a dilution effect, indicating that anthropogenic aerosols in the mountain atmospheres during the nonevent period largely originated from local/regional sources rather than from long-range transport. Trehalose, a metabolism product enriched in biota in dry conditions, was 62 ± 78 and 421 ± 181 ng m−3 at Mt. Hua and Mt. Tai during DS II, 10–30 times higher than that in the nonevent time, indicating that trehalose may be a tracer for dust emissions from Gobi desert regions. Molecular compositions of organic aerosols in the mountain samples demonstrate that domestic coal burning is still the major source of PAHs in China. n-Alkanes and fatty acids showed a bimodal size distribution during the nonevent with a major peak in fine mode (2.1 μm). The coarse mode significantly increased and even dominated over the whole size range when dust was present. Glucose and trehalose were also dominant in the coarse mode especially in the DS II time. PAHs and levoglucosan concentrated in fine particles with no significant changes in size distribution when dust storm occurred. However, phthalic and succinic acids showed bimodal size distribution pattern with an increase in coarse mode during the event, because both are formed via a gas phase oxidation and a subsequent condensation/adsorption onto aerosol phase. In contrast, terephthalic and malic acids are mostly emitted from combustion process as fine particles, thus both showed a fine mode pattern during the whole campaign with a minor peak in coarse mode caused by an increased coagulation with dust during the event. Geometric mean diameters (GMDs) of the organic aerosols above are in general larger at Mt.~Hua than at Mt. Tai during the nonevent period. We found that during the event GMD of the fine mode organics that derived mostly from the local/regional sources rather than Gobi desert became smaller while GMD of them in coarse mode became larger. Such a splitting in sizes during the event is most likely caused by decreased fine particle coagulation due to dilution and increased adsorption/coagulation with dust.

Beschreibung: A perfluorocarbon tracer system (PERTRAS), specifically designed for Lagrangian aircraft experiments, has been developed by the Deutsches Zentrum für Luft- und Raumfahrt (German Aerospace Center, DLR). It consists of three main parts: a tracer release unit (RU), an adsorption tube sampler (ATS) and a tracer analytical system. The RU was designed for airborne tracer release experiments; meanwhile, it can be used on various platforms for different experimental purpose (here research vessel). PERTRAS was for the first time applied in the field campaign Stratospheric ozone: halogen Impacts in a Varying Atmosphere (SHIVA) in November 2011. An amount of 8.8 kg perfluoromethylcyclopentane (PMCP) was released aboard the research vessel Sonne (RV Sonne) near the operational site of this campaign, Miri, Malaysia, on 21 November. The tracer samples collected using the ATS on board the DLR research aircraft Falcon were analyzed in the laboratory using a thermal desorber/gas chromatography/mass spectrometry (TD/GC/MS) system. Guided by forecasts calculated with the Lagrangian model, Hybrid Single Particle Lagrangian Integrated Trajectory (HYSPLIT), 64 tracer samples were collected onboard the Falcon approximately 5 and 25 h after the release, respectively, mostly with a time resolution of 1 min. Enhanced PMCP concentrations relative to ambient PMCP background values (mean: 6.62 fmol mol−1) were detected during three intersects of the fresh tracer plume (age 5 h), with a maximum value of 301.33 fmol mol−1. This indicates that the fresh tracer plume was successfully intercepted at the forecasted position. During the second flight, 25 h after the release, the center of tracer plume was not detected by the sampling system due to a faster advection of the plume than forecasted. The newly developed PERTRAS system has been successfully deployed for the first time. The instrumental set-up and comparisons between the measurements and HYSPLIT simulations are presented in this study.

Beschreibung: PM10 and size-resolved particles (9-stage) were simultaneously collected at Mt. Hua and Mt. Tai in Central and East China during the spring of 2009 including a massive dust storm occurring on April 24th (named as DS II), and determined for organic compounds to investigate the impact of dust storm on organic aerosols. High molecular weight (HMW) n-alkanes, fatty acids, and fatty alcohols and trehalose sharply increased and almost entirely stayed in coarse particles when dust storm was present, suggesting that high level of organic aerosols in the mountain atmospheres during the event originated from biogenic sources in the Gobi desert. However, most anthropogenic aerosols (e.g., PAHs, aromatic acids and dicarboyxlic acids) during the event significantly decreased due to a dilution effect, indicating that anthropogenic aerosols in the mountain air during the nonevent period are largely derived from local/regional sources rather than from long-range transport. Our results indicate that trehalose can be taken as a new tracer for dust emissions from desert regions since trehalose was negligible in the nonevent but abundant in the event. Molecular compositions of organic aerosols in the mountain samples further demonstrate that domestic coal burning is still the major source of PAHs in China. n-Alkanes and fatty acids showed a bimodal size distribution during the nonevent with a major peak in fine mode (2.1 μm). The coarse mode significantly increased and even dominated over the whole size range when dust was present. Glucose and trehalose were also dominant in the coarse mode especially in the DS II time. PAHs and levoglucosan concentrated in fine particles with no significant changes in size distribution when dust storm occurred. However, phthalic and succinic acids showed bimodal size distribution pattern with an increase in coarse mode during the event, because both are formed via a gas phase oxidation and a subsequent condensation/adsorption onto aerosol phase. In contrast, terephthalic and malic acids are mostly emitted from combustion process as fine particles, thus both showed a fine mode pattern during the whole campaign with a minor peak in coarse mode caused by an increased coagulation with dust during the event. Geometric mean diameters (GMDs) of the organic aerosols above are in general larger at Mt. Hua than at Mt. Tai during the nonevent period. We found that during the event GMD of the fine mode organics that derived mostly from the local/regional sources rather than Gobi desert became smaller while GMD of them in coarse mode became larger. Such a polarization in sizes during the event is most likely caused by decreased fine particle coagulation due to dilution and increased adsorption/coagulation with dust.

Beschreibung: A longstanding puzzle in isotope studies of C3 plant species is that heterotrophic plant organs (e.g., stems, roots, seeds, and fruits) tend to be enriched in 13C compared to the autotrophic organ (leaves) that provides them with photosynthate. Our inability to explain this puzzle suggests key deficiencies in understanding post-photosynthetic metabolic processes. It also limits the effectiveness of applications of stable carbon isotope analyses in a variety of scientific disciplines ranging from plant physiology to global carbon cycle studies. To gain insight into this puzzle, we excavated whole plant architectures of Nitraria tangutorum Bobrov, a C3 species that has an exceptional capability of fixing sands and building sand dunes, in two deserts in northwestern China. We systematically and simultaneously measured carbon isotope ratios and nitrogen and phosphorous contents of different parts of the excavated plants. We also determined the seasonal variations in leaf carbon isotope ratios on nearby intact plants of N. tangutorum. We found, for the first time, that higher nitrogen contents in heterotrophic organs were significantly correlated with increased heterotrophic 13C enrichment compared to leaves. However, phosphorous contents had no effect on the enrichment. In addition, new leaves had carbon isotope ratios similar to roots but were progressively depleted in 13C as they matured. We concluded that a nitrogen-mediated process, probably the refixation of respiratory CO2 by phosphoenolpyruvate (PEP) carboxylase, was responsible for the differences in 13C enrichment among different heterotrophic organs while processes within leaves or during phloem loading may contribute to the overall autotrophic – heterotrophic difference in carbon isotope compositions.

Beschreibung: To understand the causes of the past water cycle variations and the influence of climate variability on the streamflow, lake storage, and flood potential, we analyze the changes in streamflow and the underlying drivers in four typical watersheds (Gaosha, Meigang, Saitang, and Xiashan) within the Poyang Lake Basin, based on the meteorological observations at 79 weather stations, and datasets of streamflow and river level at four hydrological stations for the period of 1961-2000. The contribution of different climate factors to the change in streamflow in each watershed is estimated quantitatively using the water balance equations. Results show that in each watershed, the annual streamflow exhibits an increasing trend from 1961–2000. The increases in streamflow by 4.80 m3 s−1 yr−1 and 1.29 m3 s−1 yr−1 at Meigang and Gaosha, respectively, are statistically significant at the 5% level. The increase in precipitation is the biggest contributor to the streamflow increment in Meigang (3.79 m3 s−1 yr−1), Gaosha (1.12 m3 s−1 yr−1), and Xiashan (1.34 m3 s−1 yr−1), while the decrease in evapotranspiration is the major factor controlling the streamflow increment in Saitang (0.19 m3 s−1 yr−1). In addition, radiation and wind contribute more than actual vapor pressure and mean temperature to the changes in evapotranspiration and streamflow for the four watersheds. For revealing the possible change of streamflow due to the future climate change, we also investigate the projected precipitation and evapotranspiration from of the Coupled Model Intercomparison Project phase 3 (CMIP3) under three greenhouse gases emission scenarios (SRESA1B, SRESA2 and SRESB1) for the period of 2061–2100. When the future changes in the soil water storage changes are assumed ignorable, the streamflow shows an uptrend with the projected increases in both precipitation and evapotranspiration (except for the SRESB1 scenario in Xiashan watershed) relative to the observed mean during 1961–2000. Furthermore, the largest increase in the streamflow is found at Meigang (+4.31%) and Xiashan (+3.84%) under the SRESA1B scenario, while the increases will occur at Saitang (+6.87%) and Gaosha (+5.15%) under the SRESB1 scenario.

Beschreibung: Water resources have a close relationship with climate. The changes of streamflow affect the exploitation and utilization of water resources directly, and the social security and the stability of ecological system. Meteorological observations at 79 weather stations, and datasets of streamflow and river level at 4 hydrological stations were collected to analyze the changes of streamflow and underlying drivers in four typical watersheds within Poyang Lake Basin during the period from 1961 to 2000. The contributions of different factors to the changes of streamflow in four typical watersheds were quantitatively quantified using water balance equation. Then, the possible future change of streamflow was assessed using precipitation and evaporation projected by different GCMs under three different emission scenarios, including medium greenhouse gases emission scenario (SRESA1B), high greenhouse gases emission scenario (SRESA2), and low greenhouse gases emission scenario (SRESB1). The change of streamflow exhibited different characteristics the four watersheds exist different increasing trends during 1961 to 2000. The increase in streamflow in Meigang and Gaosha watersheds was at the 5% significance level, with increasing rate of 4.80 m3 s−1 yr−1 and 1.29 m3 s−1 yr−1, respectively. The increase in precipitation is the biggest contributor to streamflow increment in Meigang Gaosha, and Xiashan watersheds, while the decrease in evaporation is the major explainer for streamflow increment in Saitang watershed. Radiation and wind have larger contributions than actual vapor pressure and mean temperature to evaporation and streamflow. If soil water storage will not change in the future, with the increasing precipitation and the decreasing evaporation (not including the SRESB1 in Xiashan watershed), the streamflow shows an uptrend. Furthermore, the largest increase of Meigang watershed (+4.13%) and Xiashan watershed (+3.84%) appear under SRESA1B scenario while the increase of Saitang watershed (+6.87%) and Gaosha watershed (+5.15%) in SRESB1 scenario.

Beschreibung: In the current work TSP sample was hourly collected in Xi'an, an inland mega-city of China near the Loess Plateau, during a dust storm event of 2013 (9 March 18:00–12 March 10:00 LT), along with a size-resolved aerosol sampling and an online measurement of PM2.5. The TSP and size-resolved samples were determined for EC, OC, water-soluble organic carbon (WSOC) and nitrogen (WSON), inorganic ions and elements to investigate aerosol chemistry evolution. Hourly concentrations of Cl−, NO3−, SO42−, Na+ and Ca2+ in the TSP samples reached up to 34, 12, 180, 72 and 28 μg m−3, respectively, when dust peak arrived over Xi'an. Chemical compositions of the TSP samples showed that NH4+ and NO3− strongly correlated each other in the whole observation period (r2=0.76), while SO42− and Cl− well correlated with Na+, Ca2+, Mg2+ and K+ (r2〉0.85). Size distributions of NH4+ and NO3− presented a same pattern, which dominated in the coarse mode (〉2.1 μm during the event and predominated in the fine mode (

Beschreibung: A perfluorocarbon tracer system (PERTRAS), specifically designed for Lagrangian aircraft experiments, has been developed by the Deutsches Zentrum für Luft- und Raumfahrt (German Aerospace Center, DLR). It consists of three main parts: a tracer release unit (RU), an adsorption tube sampler (ATS), and a tracer analytical system. The RU was designed for airborne tracer release experiments; meanwhile, it can be used on various platforms for different experimental purposes (here research vessel). PERTRAS was for the first time applied in the field campaign Stratospheric ozone: Halogen Impacts in a Varying Atmosphere (SHIVA) in November 2011. An amount of 8.8 kg perfluoromethylcyclopentane (PMCP) was released aboard the research vessel Sonne (RV Sonne) near the operational site of this campaign, Miri, Malaysia, on 21 November. The tracer samples collected using the ATS onboard the DLR research aircraft Falcon were analyzed in the laboratory using a thermal desorber–gas chromatography–mass spectrometry (TD–GC–MS) system. Guided by forecasts calculated with the Lagrangian model Hybrid Single Particle Lagrangian Integrated Trajectory (HYSPLIT), 64 tracer samples were collected onboard the Falcon approximately 5 and 25 h after the release, mostly with a time resolution of 1 min. Enhanced PMCP concentrations relative to ambient PMCP background values (mean: 6.62 fmol mol−1) were detected during three intersects of the fresh tracer plume (age 5 h), with a maximum value of 301.33 fmol mol−1. This indicates that the fresh tracer plume was successfully intercepted at the forecast position. During the second flight, 25 h after the release, the center of tracer plume was not detected by the sampling system due to a faster advection of the plume than forecast. The newly developed PERTRAS system has been successfully deployed for the first time. The instrumental setup and comparisons between the measurements and HYSPLIT simulations are presented in this study.

Beschreibung: A longstanding puzzle in isotope studies of C3 plant species is that heterotrophic plant organs (e.g., stems, roots, seeds, and fruits) tend to be enriched in 13C compared to the autotrophic organ (leaves) that provides them with photosynthate. Our inability to explain this puzzle suggests key deficiencies in understanding post-photosynthetic metabolic processes. It also limits the effectiveness of applications of stable carbon isotope analyses in a variety of scientific disciplines ranging from plant physiology to global carbon cycle studies. To gain insight into this puzzle, we excavated whole plant architectures of Nitraria tangutorum Bobrov, a C3 species that has an exceptional capability of fixing sands and building sand dunes, in two deserts in northwestern China. We systematically and simultaneously measured carbon isotope ratios and nitrogen and phosphorous contents of different parts of the excavated plants. We also determined the seasonal variations in leaf carbon isotope ratios on nearby intact plants of N. tangutorum. We found, for the first time, that higher nitrogen contents in heterotrophic organs were significantly correlated with increased heterotrophic 13C enrichment compared to leaves. However, phosphorous contents had no effect on the enrichment. In addition, new leaves had carbon isotope ratios similar to roots but were progressively depleted in 13C as they matured. We concluded that a nitrogen-mediated process, hypothesized to be the refixation of respiratory CO2 by phosphoenolpyruvate (PEP) carboxylase, was responsible for the differences in 13C enrichment among different heterotrophic organs, while processes such as fractionating foliar metabolism and preferentially loading into phloem of 13C-enriched sugars may contribute to the overall autotrophic–heterotrophic difference in carbon isotope compositions.

Beschreibung: A total suspended particulate (TSP) sample was collected hourly in Xi'an, an inland megacity of China near the Loess Plateau, during a dust storm event of 2013 (9 March 18:00−12 March 10:00 LT), along with a size-resolved aerosol sampling and an online measurement of PM2.5. The TSP and size-resolved samples were determined for elemental carbon (EC), organic carbon (OC), water-soluble organic carbon (WSOC) and nitrogen (WSON), inorganic ions and elements to investigate chemistry evolution of dust particles. Hourly concentrations of Cl−, NO3−, SO42−, Na+ and Ca2+ in the TSP samples reached up to 34, 12, 180, 72 and 28 μg m−3, respectively, when dust peak arrived over Xi'an. Chemical compositions of the TSP samples showed that during the whole observation period NH4+ and NO3− were linearly correlated with each other (r2=0.76) with a molar ratio of 1 : 1, while SO42− and Cl− were well correlated with Na+, Ca2+, Mg2+ and K+ (r2 〉 0.85). Size distributions of NH4+ and NO3− presented a same pattern, which dominated in the coarse mode (〉 2.1 μm) during the event and predominated in the fine mode (〈 2.1 μm) during the non-event. SO42− and Cl− also dominated in the coarse mode during the event hours, but both exhibited two equivalent peaks in both the fine and the coarse modes during the non-event, due to the fine-mode accumulations of secondarily produced SO42− and biomass-burning-emitted Cl- and the coarse-mode enrichments of urban soil-derived SO42− and Cl−. Linear fit regression analysis further indicated that SO42− and Cl− in the dust samples possibly exist as Na2SO4, CaSO4 and NaCl, which directly originated from Gobi desert surface soil, while NH4+ and NO3− in the dust samples exist as NH4NO3. We propose a mechanism to explain these observations in which aqueous phase of dust particle surface is formed via uptake of water vapor by hygroscopic salts such as Na2SO4 and NaCl, followed by heterogeneous formation of nitrate on the liquid phase and subsequent absorption of ammonia. Our data indicate that 54 ± 20% and 60 ± 23% of NH4+ and NO3− during the dust period were secondarily produced via this pathway, with the remaining derived from the Gobi desert and Loess Plateau, while SO42− in the event almost entirely originated from the desert regions. Such cases are different from those in the East Asian continental outflow region, where during Asia dust storm events SO42− is secondarily produced and concentrates in sub-micrometer particles as (NH4)2SO4 and/or NH4HSO4. To the best of our knowledge, the current work for the first time revealed an infant state of the East Asian dust ageing process in the regions near the source, which is helpful for researchers to understand the panorama of East Asian dust ageing process from the desert area to the downwind region.